1454573-53-5

Upstream product

• 86650-50-2 1-pentynylzinc chloride 
• 1454573-52-4 (S)-(-)-ethyl 4-hydroxynon-5-ynoate 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 627-19-0 1-Pentyne 
• 1454573-51-3 ethyl 4-oxonon-5-ynoate 
• 14794-31-1 ethyl 3-(chloroformyl)propionate 

Downstream Products

• 1454573-57-9 (S)-(-)-ethyl 4-(t-butyldiphenylsilyloxy)-4-(4-propylfuran-3-yl)butyrate 
• 1454573-58-0 (S)-(-)-4-(t-butyldiphenylsilyloxy)-4-(4-propylfuran-3-yl)butyric acid 
• 1454573-59-1 (S)-(-)-4-(t-butyldiphenylsilyloxy)-3-propyl-5,6-dihydrobenzo-7(4H)-furanone 
• 1026364-89-5 (S)-((S)-5,6-dihydro-4-hydroxy-3-propyl-7(4H)-benzofuranyl)-3,3,3-trifluoro-2-methoxy-2-phenylpropanoate 
• 1454573-60-4 (R)-((S)-5,6-dihydro-4-hydroxy-3-propyl-7(4H)-benzofuranyl)-3,3,3-trifluoro-2-methoxy-2-phenylpropanoate 

Relevant academic research and scientific papers

Concise total synthesis of (-)-auxofuran by a click Diels-Alder strategy

The first synthesis of auxofuran, a newly discovered auxin-like signaling molecule of streptomycetes, has been achieved in seven steps and 59% overall yield from commercial starting materials. Central to the synthetic route is a click-unclick Diels-Alder